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Urinary tract infections are becoming multi-drug resistant due to extended spectrum beta-lactamases-producing klebsiella pneumonia

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dc.contributor.author Hackman, H. K.
dc.contributor.author Annison, L.
dc.contributor.author Arhin, R. E.
dc.contributor.author Azumah, B. K.
dc.contributor.author Boateng, D.
dc.contributor.author Nwosu, B.
dc.date.accessioned 2022-09-01T09:51:21Z
dc.date.available 2022-09-01T09:51:21Z
dc.date.issued 2021
dc.identifier.other 10.1016/j.ijid.2015.03.006
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S1201971215000673
dc.identifier.uri http://atuspace.atu.edu.gh:8080/handle/123456789/180
dc.description.abstract Introduction: Klebsiella pneumoniae are among the most common cause of urinary tract infections such as cystitis and pyelonephritis. These multi-drug resistant K. pneumoniae are producers of extended spectrum beta-lactamases (ESBL) that are capable of hydrolyzing beta-lactams and non-beta-lactams. This laboratory-based study sought to establish the increase of ESBL-producing K. pneumoniae in multi-drug resistant urinary tract infections and determine the effective antibiotic treatment options. Methods: One hundred and seventy five K. pneumoniae isolates obtained from urine cultures were randomly collected and the combined disc synergy method was used to determine the ESBL-producing K. pneumoniae. The Vitek 2 system (bioMérieux, France) was used to perform antimicrobial susceptibility testing of 17 commonly used antibiotics. The data from the work was collated and statistically analysed using the chi-square test and Mann-Whitney U test. P values < 0.05 were considered significant. Results: Of the 175 K. pneumoniae responsible for urinary tract infections, 73.7% were producing ESBL suggesting that most urinary tract infections caused by K. pneumoniae will be multi-drug resistant. The antimicrobial resistance differences between ESBL-producing and non-ESBL-producing Klebsiella pneumoniae indicated a significance difference with p < 0.05. This study indicated that imipenem and amikacin are the antibiotic of choice for the treatment of multi-drug resistant urinary tract infections caused by ESBL-producing K. pneumoniae. Cephalosporins and nitrofurantoin are suitable for the treatment of urinary tract infections due to non-ESBL-producing K. pneumoniae. Conclusion: This study indicated that imipenem (carbapenem) and amikacin are the antibiotic of choice for the treatment of multi-drug resistant urinary tract infections caused by ESBL-producing K. pneumoniae. The third and fourth generation cephalosporins and nitrofurantoin are suitable for the treatment of urinary tract infections due to non-ESBL-producing K. pneumoniae. Rational use of antibiotics and evidence based antibiotic prescription will help to control the spread of resistance by ESBL-producing K. pneumoniae. There is the need to intensify research in the use of natural products to treat multi-drug resistant urinary tract infections emanating from ESBL-producing K. pneumoniae en_US
dc.language.iso en en_US
dc.publisher Elsevier Ltd en_US
dc.relation.ispartofseries vol;6
dc.title Urinary tract infections are becoming multi-drug resistant due to extended spectrum beta-lactamases-producing klebsiella pneumonia en_US
dc.type Article en_US


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